Catalog No.:AA003CEV

39637-99-5 | (R)-(+)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride

Name: Name:(R)-(+)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride
Brand: AABLOCKS
SKU: AA003CEV
Availability: InStock
Rating: 90 (10 reviews)

Pack Size

Purity

Availability

Price(USD)

Quantity

100mg

>98.0%(GC)(T)

in stock

$63.00 $44.00

- +

>98.0%(GC)(T)

in stock

$368.00 $258.00

- +

in stock

$696.00 $488.00

- +

Technical Information
Properties
Downstream Synthesis Route
Literature
Request for Quotation
Download SDS

Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA003CEV

Chemical Name:

(R)-(+)-α-Methoxy-α-(trifluoromethyl)phenylacetyl chloride

CAS Number:

39637-99-5

Molecular Formula:

C10H8ClF3O2

Molecular Weight:

252.6175

MDL Number:

MFCD00044400

SMILES:

CO[C@@](C(F)(F)F)(c1ccccc1)C(=O)Cl

Properties

BP:

213-214 °C(lit.)

Form:

Liquid

Refractive Index:

n20/D 1.469(lit.)

Stability:

Moisture Sensitive

Storage:

Inert atmosphere;-20 ℃;

Computed Properties

Complexity:

261

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Rotatable Bond Count:

XLogP3:

3.3

Downstream Synthesis Route

73349-08-3

39637-99-5

73349-12-9

[1]Tetrahedron,1979,vol.35,p.1601-1605

39637-99-5

73349-07-2

73349-11-8

[1]Mori;Sasaki;Tamada;etal.[Tetrahedron,1979,vol.35,#13,p.1601-1605]

124602-03-5

39637-99-5

124575-34-4

124575-35-5

[1]Craven,AndrewP.;Dyke,HazelJ.;Thomas,EricJ.[Tetrahedron,1989,vol.45,#8,p.2417-2430]

2041-14-7

39637-99-5

115463-93-9

[1]LiebigsAnnalenderChemie,1988,p.961-964

24621-61-2

39637-99-5

bis-(R)-MTPAesterof(S)-(+)-1,3-butanediol

[1]Phytochemistry,1993,vol.33,p.393-396

[2]Organicletters,2001,vol.3,p.1363-1366

Literature

Title: Stereoselective method development and validation for determination of concentrations of amphetamine-type stimulants and metabolites in human urine using a simultaneous extraction-chiral derivatization approach.

Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences 20110101

Title: Development of a simultaneous liquid-liquid extraction and chiral derivatization method for stereospecific GC-MS analysis of amphetamine-type stimulants in human urine using fractional factorial design.

Journal: Biomedical chromatography : BMC 20080901

Title: Quantitative and isomeric determination of amphetamine and methamphetamine from urine using a nonprotic elution solvent and R(-)-alpha-methoxy-alpha-trifluoromethylphenylacetic acid chloride derivatization.

Journal: Journal of analytical toxicology 20051001

Title: Enantiomeric separation and quantitation of (+/-)-amphetamine, (+/-)-methamphetamine, (+/-)-MDA, (+/-)-MDMA, and (+/-)-MDEA in urine specimens by GC-EI-MS after derivatization with (R)-(-)- or (S)-(+)-alpha-methoxy-alpha-(trifluoromethy)phenylacetyl chloride (MTPA).

Journal: Journal of analytical toxicology 20040901

Title: Synthesis, resolution, and determination of the absolute configuration of the enantiomers of cis-4,5-dihydroxy-1,2-dithiane 1,1-dioxide, an HIV-1NCp7 inhibitor.

Journal: Bioorganic & medicinal chemistry 20030717

Title: Method development for the high-performance liquid chromatographic enantioseparation of 2-cyanocycloalkanols.

Journal: Journal of chromatographic science 20010501

Quotation Request

Company Name:

Contact Person:

Email:

Quantity Required:

Country:

Additional Info:

SDS